Knapp Jenny, Gottstein Bruno, Bretagne Stéphane, Bart Jean-Mathieu, Umhang Gérald, Richou Carine, Bresson-Hadni Solange, Millon Laurence
UMR CNRS 6249 Laboratoire Chrono-environnement, Université Franche-Comté, 16 Route de Gray, 25030 Besançon, France.
Department of Parasitology-Mycology, National Reference Centre for Echinococcoses, University Hospital of Besançon, 25030 Besançon, France.
Pathogens. 2020 Apr 13;9(4):282. doi: 10.3390/pathogens9040282.
For clinical epidemiology specialists, connecting the genetic diversity of to sources of infection or particular sites has become somewhat of a holy grail. It is very difficult to trace the infection history of alveolar echinococcosis (AE) patients as there may be an incubation period of five to 15 years before reliable diagnosis. Moreover, the variability of parasitic manifestations in human patients raises the possibility of genetically different isolates of having different levels of pathogenicity. Thus, the exposure of human patients to different strains or genotypes circulating in geographically different environments may lead to different disease outcomes. Molecular tools, such as the microsatellite marker EmsB, were required to investigate these aspects. This genetic marker was previously tested on a collection of 1211 European field samples predominantly of animal origin, referenced on a publicly available database. In this study, we investigated a panel of 66 metacestode samples (between 1981 and 2019) recovered surgically from 63 patients diagnosed with alveolar echinococcosis originating from four European countries (France, Switzerland, Germany, Belgium). In this study, we identified nine EmsB profiles, five of which were found in patients located in the same areas of France and Switzerland. One profile was detected on both sides of the French-Swiss border, whereas most patients from non-endemic regions clustered together in another profile. EmsB profiles appeared to remain stable over time because similar profiles were detected in patients who underwent surgery recently and patients who underwent surgery some time ago. This study sheds light on possible pathways of contamination in humans, including proximity contamination in some cases, and the dominant contamination profiles in Europe, particularly for extrahepatic lesions.
对于临床流行病学专家而言,将[某种寄生虫]的遗传多样性与感染源或特定部位联系起来,已成为某种难以实现的目标。肺泡型棘球蚴病(AE)患者的感染史很难追溯,因为在可靠诊断之前可能存在5至15年的潜伏期。此外,人类患者寄生虫表现的变异性增加了遗传上不同的[寄生虫]分离株具有不同致病水平的可能性。因此,人类患者接触地理环境不同的不同菌株或基因型可能导致不同的疾病结果。需要分子工具,如微卫星标记EmsB,来研究这些方面。这种遗传标记先前已在主要来自动物的1211份欧洲野外样本的集合上进行了测试,并参考了一个公开可用的数据库。在本研究中,我们调查了一组66个从63名诊断为肺泡型棘球蚴病的患者手术中回收的原头蚴样本(时间跨度为1981年至2019年),这些患者来自四个欧洲国家(法国、瑞士、德国、比利时)。在本研究中,我们确定了9种EmsB谱型,其中5种在法国和瑞士相同地区的患者中发现。在法瑞边境两侧检测到一种谱型,而大多数来自非流行地区的患者聚集在另一种谱型中。EmsB谱型似乎随时间保持稳定,因为在近期接受手术的患者和一段时间前接受手术的患者中检测到了相似的谱型。这项研究揭示了人类可能的污染途径,包括在某些情况下的近距离污染,以及欧洲主要的污染谱型,特别是对于肝外病变。